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Title: Measuring elastase, proteinase 3 and cathepsin G activities at the surface of human neutrophils with fluorescence resonance energy transfer substrates
Authors: Korkmaz, Brice
Attucci, Sylvie
Juliano, Maria Aparecida [UNIFESP]
Kalupov, Timofey
Jourdan, Marie-Lise
Juliano, Luiz [UNIFESP]
Gauthier, Francis
Proteases & Vectorisat Pulm Fac Med
Max Planck Inst Neurobiol
Univ Tours
Universidade Federal de São Paulo (UNIFESP)
Issue Date: 1-Jan-2008
Publisher: Nature Publishing Group
Citation: Nature Protocols. London: Nature Publishing Group, v. 3, n. 6, p. 991-1000, 2008.
Abstract: The neutrophil serine proteases (NSPs) elastase, proteinase 3 and cathepsin G are multifunctional proteases involved in pathogen destruction and the modulation of inflammatory processes. A fraction of secreted NSPs remains bound to the external plasma membrane, where they remain enzymatically active. This protocol describes the spectrofluorometric measurement of NSP activities on neutrophil surfaces using highly sensitive Abz-peptidyl-EDDnp fluorescence resonance energy transfer (FRET) substrates that fully discriminate between the three human NSPs. We describe FRET substrate synthesis, neutrophil purification and handling, and kinetic experiments on quiescent and activated cells. These are used to measure subnanomolar concentrations of membrane-bound or free NSPs in low-binding microplates and to quantify the activities of individual proteases in biological fluids like expectorations and bronchoalveolar lavages. the whole procedure, including neutrophil purification and kinetic measurements, can be done in 4-5 h and should not be longer because of the lifetime of neutrophils. Using this protocol will help identify the contributions of individual NSPs to the development of inflammatory diseases and may reveal these proteases to be targets for therapeutic inhibitors.
ISSN: 1754-2189
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